Director of R&D Engineering

About UsAt Sila, we are pioneering the development of next-generation battery materials aimed at revolutionizing clean energy. Our mission centers on engineering advanced lithium-ion batteries that enhance energy density while minimizing size and weight. By creating smaller, more powerful batteries, we are driving innovation across consumer electronics and a…

Join Penumbra Inc. as a Senior Business Systems Analyst focused on Customer Relationship Management (CRM). In this pivotal role, you will leverage your expertise to enhance our CRM strategies, ensuring optimal alignment with our business objectives. Collaborate with cross-functional teams to drive system improvements, support user needs, and facilitate training initiatives.

About UsAt Sila Nanotechnologies, we are at the forefront of revolutionizing battery materials to accelerate the global transition to clean energy. Our team is dedicated to engineering and manufacturing innovative lithium-ion battery materials that enhance energy density while minimizing size and weight. By creating smaller, more powerful batteries, we are enabling advancements in consumer technology and fostering the widespread adoption of electric vehicles, thus reducing reliance on fossil fuels. Join us as we confront one of the greatest challenges of our era and redefine the limits of possibility.Who You AreAs a Senior ERP Finance Consultant specializing in Sage X3, you will be pivotal in aligning our Finance department with our Data Systems and ERP teams. Your expertise in Sage X3 Finance modules will enable you to serve as a subject matter expert (SME) and facilitate seamless end-to-end financial processes, ensuring system accuracy, compliance, and operational efficiency. This role is a temporary consulting opportunity.

Join Penumbra as a Quality Engineer and play a pivotal role in ensuring the quality and safety of our revolutionary medical devices designed to tackle some of the most challenging health conditions globally. You will engage with complex, technical challenges that require innovative solutions, influencing every phase from initial concept through commercialization, and driving continual enhancements. Your passion for creative problem-solving will be vital as you contribute to the well-being of patients worldwide.

OverviewJoin our innovative team at Penumbra, Inc., where you will play a pivotal role in ensuring the production of high-quality, life-saving medical devices. As a Senior Quality Engineer, you will independently manage significant projects, collaborating closely with Commercial Operations to uphold the highest standards in the manufacturing of Class II/III interventional medical devices. This position challenges you to analyze complex problems, leveraging your expertise to make informed decisions regarding quality actions and to communicate and implement quality objectives effectively.Key Responsibilities• Collaborate with Commercial Operations and Manufacturing teams on activities such as Incoming/In-process/Final Inspections, Non-Conformance Reports (NCRs), Corrective and Preventive Actions (CAPAs), Engineering Change Orders, Control Chart Investigations, Deviation Authorizations, and equipment maintenance tasks.• Support specific product lines by performing failure analyses and investigating defects as necessary.• Drive Continuous Improvement initiatives and collaborate on their execution.• Engage in supplier-related activities including Second Source Qualifications, Supplier Changes, and Supplier Corrective Action Requests (SCARs).• Work closely with engineering departments and suppliers to address quality-related concerns.• Lead or contribute to the development of manufacturing documentation.• Design, enhance, and support test methodologies, testing equipment, and test method validations (TMVs).• Suggest updates to specifications, acceptance criteria, and manufacturing documents to enhance product quality and operational efficiency.• Mentor junior Quality Engineers, providing guidance in departmental functions.• Fulfill responsibilities outlined by the Quality Management System (QMS) and perform additional duties as assigned.• Ensure departmental compliance with QMS, regulations, standards, and procedures.• Execute other work-related tasks as directed.QualificationsMinimum Education and Experience:• Associate's or Bachelor's degree in Engineering, Life Sciences, or a related field with a minimum of 3 years of relevant experience in quality engineering, preferably within the medical device industry, or an equivalent combination of education and experience.Additional Qualifications:• Strong knowledge of QSR, ISO, and applicable regulations and standards is essential.• Exceptional verbal, written, and interpersonal communication skills are required.• Demonstrated leadership abilities are preferred.• Proficiency in MS Office Suite (Word, Excel, PowerPoint) is required.Working Environment• The role is situated in general office, laboratory, and cleanroom settings, promoting a collaborative and innovative atmosphere.

OverviewJoin our dynamic team at Penumbra, Inc. as a Manager of Quality Engineering, where you will spearhead a talented group of Quality Engineers dedicated to enhancing the manufacturing operations and production lines for our innovative range of medical devices. Your leadership will be pivotal in ensuring the highest standards of manufacturing quality performance, developing effective inspection strategies, optimizing yield, and maintaining robust process controls throughout the product lifecycle, from initial commercial ramp-up to product maturity and site transfer.As a key member of our Technical Operations team, you will collaborate closely with Manufacturing Engineering, Production, and Industrial Engineering to embed quality into the manufacturing processes from the outset. With a commitment to quality excellence, you will implement effective process controls, inspection strategies, and data-driven monitoring to mitigate risks. Your efforts will directly contribute to improved product yield, enhanced productivity, and operational stability by preventing defects, identifying issues at their inception, and ensuring a consistent, compliant manufacturing performance.Key Responsibilities• Provide leadership for Quality Engineering across assigned product portfolios and production lines.• Act as the primary quality liaison for Production, Manufacturing Engineering, and Industrial Engineering.• Oversee manufacturing quality performance metrics, including yield, scrap, productivity, and throughput-related quality losses.• Develop and refine comprehensive inspection strategies, including in-process checks, final inspections, destructive testing, sampling plans, and acceptance/rejection criteria.• Initiate and lead continuous improvements in inspection systems, testing methodologies, process monitoring, and digital quality tools.• Employ Lean and Six Sigma principles to enhance yield, minimize waste, and improve process capability.• Manage quality system activities within Operations, including Non-Conformance Reports (NCRs), Material Review Board (MRB) activities, Corrective and Preventive Actions (CAPAs), control chart investigations, and effectiveness verification.• Advocate for process-based risk management, including performing process Failure Mode and Effects Analyses (pFMEAs) and defining Critical to Quality (CTQ) metrics.• Review and endorse equipment-related quality tasks, such as equipment qualifications (IQ/OQ), equipment change orders (ECOs), non-standard maintenance activities, and equipment software validation, in collaboration with Manufacturing Engineering.• Recruit, develop, and manage a team of Quality Engineers, overseeing workload and FTE planning to align with production priorities.*Essential functions of the role.

THE COMPANYSaildrone is a pioneering maritime defense organization and the foremost authority in autonomous unmanned surface vehicles (USVs). With unparalleled experience traversing ocean miles and real-world operations, Saildrone actively supports national security and force projection globally, 24/7/365.Our manufacturing and R&D headquarters are situated in Alameda, CA, complemented by business development and sales operations in Washington, DC, and deployment hubs across Europe and the Middle East. By integrating proven autonomous operations, edge computing, advanced sensing, renewable energy, and cutting-edge unmanned surface technology, Saildrone is redefining the operational capabilities of future naval forces. Come be a part of a dynamic, mission-driven team at the forefront of maritime security and autonomous innovation.THE POSITIONWe are looking for a Senior Operations Quality Manager to enhance our Operations Team. Reporting directly to the Chief Operating Officer, you will spearhead the daily execution and evolution of our Quality Management System, ensuring that every vehicle delivered meets the highest standards of reliability, traceability, and performance. As production scales and product complexity increases, you will guarantee that our quality systems advance in tandem with the business—from supplier qualifications through manufacturing, deployment, and fleet operations. We seek a hands-on technical leader adept at creating clarity from ambiguity, driving disciplined follow-through, and possessing a proven history of successful execution in fast-paced hardware environments.THE TEAMThe Operations Team oversees the manufacturing, deployment, and maintenance of Saildrone’s autonomous surface vehicles. We develop and uphold the operational infrastructure necessary to ensure global maritime domain awareness within a national security and defense framework. Quality is central to this mission—connecting manufacturing and field service to swiftly identify issues, thoroughly resolve root causes, and close feedback loops efficiently. This role collaborates across Engineering, Supply Chain, Production, and Technical Operations to maintain rigor as we scale.THE RESPONSIBILITIESMature and expand the Quality Management System (QMS) to achieve ISO9001 and/or AS9100D compliance, overseeing internal/external audits, documentation controls, and traceability systems to meet stringent certification criteria.Establish and manage company-wide quality KPIs (e.g., First Pass Yield, defect rate, cost of quality) and reporting dashboards to provide...

General SummaryThe Quality Engineer II plays a crucial role in developing and executing robust quality system elements to uphold the excellence of both new and existing product lines. This position ensures compliance with pertinent regulations and standards while addressing moderate-scope problems that require in-depth analysis of identifiable factors. The engineer will exercise sound judgment to determine optimal actions and effectively communicate and implement quality objectives across the organization.Specific Duties and Responsibilities• Collaborate in the development and qualification processes for both new and existing products.• Develop comprehensive testing and inspection methodologies along with associated documentation.• Engage actively with Quality Objective teams.• Design and implement Quality Control (QC) process sampling systems, procedures, and statistical techniques.• Specify or design inspection and testing mechanisms and equipment tailored for product requirements.• Conduct failure analyses and defect investigations to enhance product quality.• Analyze production limitations and standards to recommend improvements.• Suggest revisions to specifications to align with quality standards.• Interface effectively with engineering departments, customers, and suppliers on quality-related issues.• Assist in the creation of standard operating procedures (SOPs).• Facilitate and conduct internal audits to ensure compliance.• Adhere to the Company's Quality Management System (QMS) and global quality regulations and standards.• Understand and comply with relevant security, privacy, and compliance principles.• Ensure adherence to QMS, regulations, standards, and procedures within the department.• Undertake additional work-related duties as assigned.*Indicates essential functions of the role.Location and Salary:• Location: Alameda, CA• Salary: $95,000 to $127,000• Compensation is subject to variation based on performance, skill level, competencies, work location, and shift.Position QualificationsMinimum education and experience: • Associate’s or Bachelor's degree in Engineering, Life Sciences, or a related field, with a minimum of 2 years of relevant experience in quality engineering, preferably within the medical devices or regulated industry, or an equivalent combination of education and experience.Additional Qualifications:• Strong familiarity with Quality System Regulations (QSR), ISO standards, and other applicable regulations and laws related to quality engineering.

OverviewWe are seeking a skilled and experienced Senior Quality Engineer to join our dynamic team at Penumbra Inc. in Alameda, CA. In this pivotal role, you will leverage your engineering expertise to drive quality assurance processes and enhance product reliability. You will be responsible for planning and executing quality initiatives, utilizing your judgment and independent evaluation skills to adapt and refine standard techniques. This position requires innovative problem-solving to overcome engineering challenges and uphold our high-quality standards in manufacturing and design control.Key Responsibilities• Engage in the development and qualification of both new and existing products, ensuring they meet rigorous quality standards.*• Lead project teams to synchronize quality efforts in designing, developing, and continuously enhancing products. This includes planning, scheduling, and coordinating detailed engineering phases for diverse projects.*• Conduct engineering tasks that involve conventional practices while addressing complex features such as conflicting design requirements and material unsuitability.*• Design and implement inspection, testing, and evaluation methods for precision and accuracy of equipment.• Develop and validate measurement methodologies to ensure product compliance.• Oversee design control processes to guarantee new products adhere to guidelines and maintain success metrics in alignment with regulatory standards.• Analyze product reports and returns, recommending corrective and preventive actions to enhance quality.*• Perform statistical analyses to identify accountability for products and materials failing to meet standards.*• Participate in Non-Conformance Report (NCR) and Corrective and Preventive Action (CAPA) boards as required.*• Conduct Quality System Regulation (QSR) training sessions.*• Assist during FDA inspections, FDB inspections, and notified body audits.*• Collaborate in formulating standard operating procedures.*• Prepare documentation for inspection and testing methods.*• Fulfill responsibilities associated with the Quality System and undertake additional duties as assigned.• Mentor and develop team members, setting objectives and providing ongoing feedback through performance reviews.*• Comply with the Company’s Quality Management System (QMS) and relevant domestic and international regulations.*

Join Genefab's Quality Control Analytical group as a Senior Analyst II, where your expertise will be pivotal in supporting our Good Manufacturing Practices (GMP) Quality Control testing. You will be responsible for method transfer, qualification, troubleshooting, and conducting thorough investigations. This role demands a keen analytical mindset and a commitment to maintaining the highest quality standards.

At Anthro Energy, we are pioneering the development of cutting-edge electrolytes that will revolutionize lithium-ion battery performance, enhancing safety and efficiency. We are currently on the lookout for a highly skilled and motivated Lead Staff Electrolyte Scientist to spearhead innovative electrolyte solutions, focusing on advanced cell chemistries such as high-Ni, high-voltage NCM, and silicon-dominant anodes.This is a pivotal position for a technical leader who will define and implement electrolyte strategies, tackle critical interfacial challenges, and transform innovative formulations into commercially viable battery systems. You will work at the forefront of electrolyte science, managing projects from foundational design through thorough validation in full cells and commercial integration.Key Responsibilities:Develop and refine the electrolyte formulation strategy for cutting-edge lithium-ion systems, emphasizing high-energy-density and high-voltage chemistries.Design and innovate advanced electrolyte systems, incorporating state-of-the-art additive packages and next-gen formulations optimized for Si-rich anodes and high-Ni cathodes.Address complex interfacial challenges (including SEI/CEI stability, gas evolution, impedance growth, and transition metal dissolution) under demanding operating conditions to ensure long cycle life, rapid charging capabilities, and enhanced safety performance.Drive in-depth mechanistic understanding through a combination of electrochemical techniques and advanced analytical methods, linking molecular design to cell-level behavior.Collaborate closely with cell engineering and materials teams to achieve optimal electrolyte, electrode, and cell design.Lead electrolyte initiatives within commercial programs, ensuring alignment with client needs and manufacturability considerations.Establish technical direction, create experimental frameworks, and enhance data quality and rigor across electrolyte development efforts.Contribute to intellectual property generation and technical differentiation, shaping Anthro’s long-term technology roadmap.